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      IF38.079!助力過敏性哮喘的治療研究,轉(zhuǎn)染試劑榮登《Cell Discovery》

      全球哮喘患者已超3億,其中嚴(yán)重嗜酸性粒細(xì)胞性哮喘(severe eosinophilic asthma, SEA)以嗜酸性粒細(xì)胞炎癥為主要特征,是難治性哮喘的主要表型。并且嗜酸性粒細(xì)胞與哮喘急性發(fā)作頻率的增加以及肺功能下降密切相關(guān)。因此,靶向嗜酸性粒細(xì)胞是治療SEA的潛在策略。
       2022年8月16日,浙江大學(xué)醫(yī)學(xué)院應(yīng)頌敏、沈華浩教授團(tuán)隊在《Cell Discovery》期刊(IF:38.079)在線發(fā)表了題為《Treatment of allergic eosinophilic asthma through engineered IL-5-anchored chimeric antigen receptor T cells》的研究論文。研究發(fā)現(xiàn)IL-5-anchored CCAR-T (簡稱CCAR-T)細(xì)胞能夠有效抑制氣道中炎癥因子的分泌和炎癥細(xì)胞的浸潤,具有明顯的緩解作用。揭示了CCAR-T細(xì)胞在體內(nèi)外對嗜酸性粒細(xì)胞的靶向殺傷作用以及對過敏性氣道炎癥的保護(hù)作用,為過敏性哮喘的治療研究提供了潛在新的策略。

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      在該研究中,研究團(tuán)隊選擇了翌圣的轉(zhuǎn)染試劑Polybrene(聚凝胺)用于逆轉(zhuǎn)錄病毒介導(dǎo)的的T細(xì)胞基因轉(zhuǎn)染研究:

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      目前翌圣轉(zhuǎn)染試劑系列的產(chǎn)品已經(jīng)榮登Nature》、《Cell》等多個頂級期刊,獲得科研大牛們的認(rèn)可!
      IF55分!翌圣轉(zhuǎn)染試劑助力高分文章

      翌圣明星CP--轉(zhuǎn)染試劑與PCR產(chǎn)品又登《Cell》期刊

      超燃!翌圣轉(zhuǎn)染試劑助力這個團(tuán)隊連發(fā)3篇IF10+文章

      翌圣轉(zhuǎn)染試劑助力發(fā)文254篇,累積IF達(dá)2000+

      以下僅展示部分論文:

      [1] Liu R, Yang J, Yao J, et al. Optogenetic control of RNA function and metabolism using engineered light-switchable RNA-binding proteins. Nat Biotechnol. 2022;40(5):779-786. doi:10.1038/s41587-021-01112-1(IF=68.164)

      [2] Luo J, Yang Q, Zhang X, et al. TFPI is a colonic crypt receptor for TcdB from hypervirulent clade 2 C. difficile. Cell. 2022;185(6):980-994.e15. doi:10.1016/j.cell.2022.02.010 (IF=66.85)

      [3] Zhou J, Chen P, Wang H, et al. Cas12a variants designed for lower genome-wide off-target effect through stringent PAM recognition. Mol Ther. 2022;30(1):244-255. doi:10.1016/j.ymthe. 2021.10.010 (IF=12.910)

      [4] Chen S, Cao X, Zhang J, Wu W, Zhang B, Zhao F. circVAMP3 Drives CAPRIN1 Phase Separation and Inhibits Hepatocellular Carcinoma by Suppressing c-Myc Translation. Adv Sci (Weinh). 2022;9(8):e2103817. doi:10.1002/advs.202103817 (IF=17.694)

      [5] Zhang Y, Yu X, Sun R, et al. Splicing factor arginine/serine-rich 8 promotes multiple myeloma malignancy and bone lesion through alternative splicing of CACYBP and exosome-based cellular communication. Clin Transl Med. 2022;12(2):e684. doi:10.1002/ctm2.684 (IF=11.492)

      [6] Qin J, Cai Y, Xu Z, et al. Molecular mechanism of agonism and inverse agonism in ghrelin receptor. Nat Commun. 2022;13(1):300. Published 2022 Jan 13. doi:10.1038/s41467-022-27975-9 (IF=17.681)

      [7] Tang X, Deng Z, Ding P, et al. A novel protein encoded by circHNRNPU promotes multiple myeloma progression by regulating the bone marrow microenvironment and alternative splicing. J Exp Clin Cancer Res. 2022;41(1):85. Published 2022 Mar 8. doi:10.1186/s13046-022-02276-7(IF=12.658)

      [8] Yang X, Wang X, Xu Z, et al. Molecular mechanism of allosteric modulation for the cannabinoid receptor CB1 [published online ahead of print, 2022 May 30]. Nat Chem Biol. 2022;10.1038/s41589-022-01038-y. doi:10.1038/s41589-022-01038-y (IF=16.174)

      [9] Xie F, Su P, Pan T, et al. Engineering Extracellular Vesicles Enriched with Palmitoylated ACE2 as COVID-19 Therapy. Adv Mater. 2021;33(49):e2103471. doi:10.1002/adma. 202103471 (IF=30.849)

      [10] Liang Y, Lu Q, Li W, et al. Reactivation of tumour suppressor in breast cancer by enhancer switching through NamiRNA network. Nucleic Acids Res. 2021;49(15):8556-8572. doi:10.1093/nar/gkab626 (IF=16.9)

      [11] Fan Y, Wang J, Jin W, et al. CircNR3C2 promotes HRD1-mediated tumor-suppressive effect via sponging miR-513a-3p in triple-negative breast cancer. Mol Cancer. 2021;20(1):25. Published 2021 Feb 2. doi:10.1186/s12943-021-01321-x (IF=27.403)

      [12] Dai L, Dai Y, Han J, et al. Structural insight into BRCA1-BARD1 complex recruitment to damaged chromatin. Mol Cell. 2021;81(13):2765-2777.e6. doi:10.1016/j.molcel.2021.05.010 (IF=17.97)

      [13] Zhang K, Wang A, Zhong K, et al. UBQLN2-HSP70 axis reduces poly-Gly-Ala aggregates and alleviates behavioral defects in the C9ORF72 animal model. Neuron. 2021;109(12):1949-1962.e6. doi:10.1016/j.neuron.2021.04.023 (IF=17.17)

      [14] Liang Y, Lu Q, Li W, et al. Reactivation of tumour suppressor in breast cancer by enhancer switching through NamiRNA network. Nucleic Acids Res. 2021;49(15):8556-8572. doi:10.1093/nar/gkab626 (IF=16.9)

      [15] Li T, Chen X, Qian Y, et al. A synthetic BRET-based optogenetic device for pulsatile transgene expression enabling glucose homeostasis in mice. Nat Commun. 2021;12(1):615. Published 2021 Jan 27. doi:10.1038/s41467-021-20913-1 (IF=14.92)

      [17] Gu C, Wang Y, Zhang L, et al. AHSA1 is a promising therapeutic target for cellular proliferation and proteasome inhibitor resistance in multiple myeloma. J Exp Clin Cancer Res. 2022;41(1):11. Published 2022 Jan 6. doi:10.1186/s13046-021-02220-1 (IF=11.161)

      [18] Zhou Y, Li D, Luo J, et al. Sulfated glycosaminoglycans and low-density lipoprotein receptor mediate the cellular entry of Clostridium novyi alpha-toxin. Cell Res. 2021;31(8):935-938. doi:10.1038/s41422-021-00510-z (IF=25.617)

      [19] Luo Q, Wu X, Zhao P, et al. OTUD1 Activates Caspase-Independent and Caspase-Dependent Apoptosis by Promoting AIF Nuclear Translocation and MCL1 Degradation. Adv Sci (Weinh). 2021;8(8):2002874. Published 2021 Feb 8. doi:10.1002/advs.202002874 (IF=15.84)

      [20] Yan F, Huang C, Wang X, et al. Threonine ADP-Ribosylation of Ubiquitin by a Bacterial Effector Family Blocks Host Ubiquitination. Mol Cell. 2020;78(4):641-652.e9. doi:10.1016/j.molcel.2020.03.016 (IF=17.97)

      [21] Sun X, Peng X, Cao Y, Zhou Y, Sun Y. ADNP promotes neural differentiation by modulating Wnt/β-catenin signaling. Nat Commun. 2020;11(1):2984. Published 2020 Jun 12. doi:10.1038/s41467-020-16799-0 (IF=14.911)

      [22] Yang X, Wang H, Xie E, et al. Rewiring ERBB3 and ERK signaling confers resistance to FGFR1 inhibition in gastrointestinal cancer harbored an ERBB3-E928G mutation. Protein Cell. 2020;11(12):915-920. doi:10.1007/s13238-020-00749-z (IF=14.872)

      [23] Zou Y, Wang A, Shi M, et al. Analysis of redox landscapes and dynamics in living cells and in vivo using genetically encoded fluorescent sensors. Nat Protoc. 2018;13(10):2362-2386. doi:10.1038/s41596-018-0042-5 (IF=13.490)

      [24] Hao H, Hu S, Chen H, et al. Loss of Endothelial CXCR7 Impairs Vascular Homeostasis and Cardiac Remodeling After Myocardial Infarction: Implications for Cardiovascular Drug Discovery. Circulation. 2017;135(13):1253-1264. doi:10.1161/CIRCULATIONAHA.116.023027 (IF=18.881)

      為回饋大家對翌圣生物轉(zhuǎn)染試劑的厚愛,正在進(jìn)行包括轉(zhuǎn)染試劑在內(nèi)的細(xì)胞類產(chǎn)品的促銷活動,請直接與當(dāng)?shù)劁N售聯(lián)系獲取最新促銷信息。 

      翌圣生物轉(zhuǎn)染試劑產(chǎn)品目錄

       

      應(yīng)用場景

      名稱

      貨號

      規(guī)格

      細(xì)胞類型:貼壁/懸浮

      核酸類型:DNA、siRNA

      Hieff Trans® 脂質(zhì)體核酸轉(zhuǎn)染試劑

      40802ES02

      0.5 mL

      40802ES03

      1.0 mL

      40802ES08

      5×1 mL

      細(xì)胞類型:貼壁/懸浮
      核酸類型:DNA

      磷酸鈣法細(xì)胞轉(zhuǎn)染試劑

      40803ES70

      200 T

      用途:病毒感染、DNA轉(zhuǎn)染

      聚凝胺(10 mg/ml

      40804ES76

      500 μL

      40804ES86

      5×500 μL

      細(xì)胞類型:懸浮
      核酸類型:DNA、siRNA

      Hieff Trans® 懸浮細(xì)胞專用脂質(zhì)體核酸轉(zhuǎn)染試劑

      40805ES02

      0.5 mL

      40805ES03

      1.0 mL

      40805ES08

      5×1 mL

      細(xì)胞類型:貼壁/懸浮
      核酸類型:siRNA、miRNA

      Hieff Trans® siRNA/miRNA體外轉(zhuǎn)染試劑

      40806ES01

      0.1 mL

      40806ES02

      0.5 mL

      40806ES03

      1.0 mL

      細(xì)胞類型:貼壁/懸浮
      核酸類型:DNA、siRNA、miRNA

      Hieff Trans® 通用型轉(zhuǎn)染試劑

      40808ES02

      0.5 mL

      40808ES03

      1 mL

      40808ES08

      5×1 mL

      細(xì)胞類型:貼壁/懸浮
      核酸類型:mRNA

      Hieff Trans® mRNA轉(zhuǎn)染試劑

      40809ES01

      0.1 mL

      40809ES03

      1 mL

      細(xì)胞類型:貼壁/懸浮
      核酸類型:DNA

      PEI轉(zhuǎn)染試劑MW25000

      40815ES03

      1 g

      40815ES08

      5×1 g

      細(xì)胞類型:貼壁/懸浮
      核酸類型:DNA

      線性PEI轉(zhuǎn)染試劑(速溶型)MW40000

      40816ES02

      100 mg

      40816ES03

      1 g

      細(xì)胞類型:293
      核酸類型:DNA
      用途:AAV/LV載體研發(fā)與工藝開發(fā)

      Hieff Trans® PEI轉(zhuǎn)染試劑

      40820ES04

      1.5 mL

      40820ES10

      10 mL

      40820ES60

      100 mL

      細(xì)胞類型:293

      核酸類型:DNA

      用途:AAV/LV載體大規(guī)模生產(chǎn)

      Hieff Trans® PEI Transfection Reagent-GMP

      40821ES10

      10 mL

      40821ES60

      100 mL

      40821ES80

      1 L


       點擊產(chǎn)品名稱查看詳情

       

       

      400-6111-883